Philureter trigoniopsis, a new genus and species (Dactylogyridae, Ancyrocephalinae) from the ureters and urinary bladder of Galaxias maculatus (Osmeriformes: Galaxiidae) in Patagonia (Argentina)

The monotypic Philureter n. gen. (Ancyrocephalinae; Dactylogyridae) is proposed to accommodate Philureter trigoniopsis n. sp. with the following features: presence of a cuplike ventral haptor armed with 14 hooks and 2 anchor/bar complexes; dorsal pair of anchors poorly defined and variable in shape, 1 frequently absent; tandem, intercecal gonads, testis bilaterally lobulated. Philureter trigoniopsis n. sp. is described from the ureters and urinary bladder of Galaxias maculatus (Jenyns, 1842) (Osmeriformes) in Patagonian Andean lakes, Argentina.     

Two new species of Cryptocephalum n. gen. (Monogenoidea: Dactylogyridae) from the cephalic lateral line of Percichthys trucha (Perciformes: Percichthyidae) in Patagonia, Argentina

Two new species of Monogenoidea were found parasitizing the cephalic lateral line canals of Percichthys trucha (Valenciennes) (Perciformes: Percichthyidae). These species are described as members of a newly proposed genus of Dactylogyridae. Cryptocephalum n. gen. is characterized by the site of infection and the combination of the several features: ventral and dorsal anchor/bar complexes, anchors with strongly elongated shaft and recurved point, shaft and point of dorsal anchors protruding laterally from haptor, hooks with 2 subunits and with pair 5 smaller than the others; gonads overlapping; coiled male copulatory organ with counterclockwise rings, accessory piece formed by 2 distinct parts, and a tubular, sclerotized ventral vagina. C ryptocephalum petreum n. sp. is characterized by having both anchor pairs protruding laterally from haptor, male copulatory organ with a coil of 2-1/2 rings, accessory piece tweezers-shaped, and sclerotized vaginal vestibule. Cryptocephalum spiralis n. sp. has ventral anchors protruding ventrally and dorsal ones protruding laterally, male copulatory organ with a coil of 1-1/2 rings, the antero-dorsal part of the accessory piece saddle-shaped, vaginal vestibule not present, and coiled vagina. This is the first record of Dactylogyridae species parasitizing the cephalic lateral line of fishes.     

Neotropical Monogenoidea. 52. Diechodactylus joaberi n. g., n. sp. from the banded knifefish Gymnotus carapo (Gymnotiformes: Gymnotidae) in southeastern Brazil

Diechodactylus joaberi n. g., n. sp. is described from the body surface of the banded knifefish Gymnotus carapo L. (Gymnotiformes: Gymnotidae) from southeastern Brazil. The new genus is proposed to accommodate species with five pairs of hooks in anterior bilateral clusters on the haptor, three pairs of hooks in a single cluster on the posterior margin of the haptor, sclerites R1 associated with the superficial bar, and confluent intestinal caeca. The presence of five pairs of hooks in two bilateral clusters anterior in the haptor permits the differentiation of species of Diechodactylus from species of all known genera of the Gyrodactylidae. The genus is likely a member of a clade of the Gyrodactylidae comprising genera with a similar hook distribution.     

Policlithrum ponticum sp. n. (Monogenea: Gyrodactylidae: Polyclithrinae) from Mugil cephalus from the Black Sea and problems of suprageneric systematics of the gydrodactylids

Polyclithrum ponticum sp. n. is described and P. mugilini Rogers, 1967 is redescribed. Both monogenean species are parasites of Mugil cephalus in the Black Sea. The new species differs from P. mugilini, P. alberti and P. boegeri by the lesser size of anchors, while it is distinguished from P. corallense by the larger size of these structures. P. ponticum sp. n. differs from all formerly described species by the greater length of dorsal connective bar. In both species from the Black Sea, "ear-like" structures situated near the external roots of anchors are described for the first time. It is suggested, that these structures take part in longitudinal, two-lobe folding of the haptor. The process of opening the haptor is probably performed by the additional bars of the haptor (bars 2 and 3 after: Rogers, 1967), joined to each other and with the anchors. The fifth pair of additional bars (Ernst e. a., 2000) derives from the "beard" of ventral connective bar and is united with its basal part. The sixth pair of additional bars (Ernst e. a., 2000) is considered as a typical "ribs" of the haptor, and therefore the "ribs" are represented by three pairs. Differences between marginal hooks of P. ponticum sp. n. and P. mugilini are insignificant, that probably depends on the presence of "ribs" of the haptor. Based on the subdivision of marginal hooks into two groups, the presence of additional supporting structure in the haptor, and the presence of the seminal receptacle, it is suggested that the subfamily Polyclithrinae Rogers, 1967 should include the genera Polyclithrum Rogers, 1967, Swingleus Rogers, 1969, Macrogyrodactylus Mamlberg, 1959, and probably Fundulotrema Hargis, 1955. Based on such characters as the lack of the anchors, the presence of suckers in the haptor, and ovipositing of eggs, it seems to be expedient to use the following taxa in systematics of gyrodactylids: Isancistrinae Fuhrmann, 1928 (genera Isancistrum, Anacanthocotyle); Gyrdicotylinae Vercammen-Grandjean, 1960 (Gyrdicotyle) and Ooegyrodactylinae Harris, 1983 (genera Phanerothecium, Ooegyrodactylus, Nothogyrodactylus, Hyperopletes).     

Neotropical Monogenoidea. 32. Cacatuocotyle paranaensis n. g., n. sp. (Dactylogyridae,Ancyrocephalinae) from Characidium spp. (Teleostei,Characidae) from the State of Paraná, Brazil

Cacatuocotyle paranaensis n. sp. (Dactylogyridae, Ancyrocephalinae) is described from the gills of the characid fishes Characidium lanei Travassos and C. pterostictum Gomes collected from two streams on the coast of the State of Paraná, Brazil. Cacatuocotyle n. g. is proposed for species possessing a single cephalic lobe (terminal), one pair of head organs, a convex haptor with thickened muscular anterior margins, one anchor-bar complex (ventral), seven pairs of ventral hooks (one pair associated with the anchor shafts; one central pair anterior to the bar; five submarginal bilateral pairs) and a sinistral vaginal aperture.     

Neotropical Monogenoidea. 33. Three new species of Ancistrohaptor n. g. (Dactylogyridae,Ancyrocephalinae) on Triportheus spp. (Teleostei,Characidae) from Brazil,with checklists of ancyrocephalines recorded from neotropical characiform fishes

Three new species of Ancistrohaptor n. g. are described from the gills of three species of Triportheus (Characidae) collected from the environs of Manaus, Amazonas, Brazil: A. falcatum n. sp. from T. elongatus; and A. falciferum n. sp. and A. falcunculum n. sp. from T. angulatus, T. albus and T. elongatus. Ancistrohaptor n. g. is proposed for species possessing overlapping gonads, a dextral or dextroventral vaginal aperture, a coiled (counter-clockwise) male copulatory organ, two accessory pieces in the copulatory complex, and a haptor armed with two pairs of anchors (ventral anchor with elongate shaft), dorsal and ventral bars and 14 hooks; hook pair 1 (ventral) anterior to ventral bar, pairs 2–4 (ventral) lying bilaterally anterior to ventral anchor bases, pair 5 (ventral) associated with distal end of ventral anchor shafts, and pairs 6 and 7 (dorsal) bilateral about midway along haptoral length. Parasite-host and host-parasite lists of the Ancyrocephalinae from neotropical Characiformes are provided.     

The family Tetraonchidae (Monogenea): its structure and position among the monogeneans

The muscle fascicles of the haptor in Tetraonchus monenteron have been described. The muscle connection of the fan-shaped dorsal bars with dorsal anchors is shown. When these muscle fascicles are contracted the dorsal anchors works as pincers. The division of tetraonchids into two genera based on types of copulatory organs, morphology of bars and haptor ans associations with different groups of fishes is restored. Different authors based on ciliated cells and chaetotaxy of the oncomiracidium and comparative spermiogenetic of T. monenteron include the tetraonchids with 16 marginal hooks into the order Dactylogyroidea. In the same time, based on the analysis of the onthogenesis of the dactylogyrid's haptor they postulate, that the haptor of these worms originally had 2 pairs of anchors and only 14 marginal hooks. The present paper contains data indicating that different representatives of the Dactylogyridea have 14-18 marginal hooks. Author put forward a suggestion, that some group of dactylogyrids originally did not have the anchors.     

On the ontogeny of the haptor and the evolution of the Monogenea

Data on the ontogeny of the posterior haptor of monogeneans were obtained from more than 150 publications and summarised. These data were plotted into diagrams showing evolutionary capacity levels based on the theory of a progressive evolution of marginal hooks, anchors and other attachment components of the posterior haptor in the Monogenea (Malmberg, 1986). 5 + 5 unhinged marginal hooks are assumed to be the most primitive monogenean haptoral condition. Thus the diagrams were founded on a 5 + 5 unhinged marginal hook evolutionary capacity level, and the evolutionary capacity levels of anchors and other haptoral attachement components were arranged according to haptoral ontogenetical sequences. In the final plotting diagram data on hosts, type of spermatozoa, oncomiracidial ciliation, sensilla pattern and protonephridial systems were also included. In this way a number of correlations were revealed. Thus, for example, the number of 5 + 5 marginal hooks correlates with the most primitive monogenean type of spermatozoon and with few sensillae, many ciliated cells and a simple protonephridial system in the oncomiracidium. On the basis of the reviewed data it is concluded that the ancient monogeneans with 5 + 5 unhinged marginal hooks were divided into two main lines, one retaining unhinged marginal hooks and the other evolving hinged marginal hooks. Both main lines have recent representatives at different marginal hook evolutionary capacity levels, i.e. monogeneans retaining a haptor with only marginal hooks. For the main line with hinged marginal hooks the name Articulon-choinea n. subclass is proposed. Members with 8 + 8 hinged marginal hooks only are here called Proanchorea n. superord. Monogeneans with unhinged marginal hooks only are here called Ananchorea n. superord. and three new families are erected for its recent members: Anonchohapteridae n. fam., Acolpentronidae n. fam. and Anacanthoridae n. fam. (with 7 + 7, 8 + 8 and 9 + 9 unhinged marginal hooks, respectively). Except for the families of Articulonchoinea (e.g. Acanthocotylidae, Gyrodactylidae, Tetraonchoididae) Bychowsky's (1957) division of the Monogenea into the Oligonchoinea and Polyonchoinea fits the proposed scheme, i.e. monogeneans with unhinged marginal hooks form one old group, the Oligonchoinea, which have 5 + 5 unhinged marginal hooks, and the other group form the Polyonchoinea, which (with the exception of the Hexabothriidae) has a greater number (7 + 7, 8 + 8 or 9 + 9) of unhinged marginal hooks. It is proposed that both these names, Oligonchoinea (sensu mihi) and Polyonchoinea (sensu mihi), will be retained on one side and Articulonchoinea placed on the other side, which reflects the early monogenean evolution. Except for the members of Ananchorea [Polyonchoinea], all members of the Oligonchoinea and Polyonchoinea have anchors, which imply that they are further evolved, i.e. have passed the 5 + 5 marginal hook evolutionary capacity level (Malmberg, 1986). There are two main types of anchors in the Monogenea: haptoral anchors, with anlages appearing in the haptor, and peduncular anchors, with anlages in the peduncle. There are two types of haptoral anchors: peripheral haptoral anchors, ontogenetically the oldest, and central haptoral anchors. Peduncular anchors, in turn, are ontogenetically younger than peripheral haptoral anchors. There may be two pairs of peduncular anchors: medial peduncular anchors, ontogentically the oldest, and lateral peduncular anchors. Only peduncular (not haptoral) anchors have anchor bars. Monogeneans with haptoral anchors are here called Mediohaptanchorea n. superord. and Laterohaptanchorea n. superord. or haptanchoreans. All oligonchoineans and the oldest polyonchoineans are haptanchoreans. Certain members of Calceostomatidae [Polyonchoinea] are the only monogeneans with both (peripheral) haptoral and peduncular anchors (one pair). These monogeneans are here called Mixanchorea n. superord. Polyonchoineans with peduncular anchors and unhinged marginal hooks are here called the Pedunculanchorea n. superord. The most primitive pedunculanchoreans have only one pair of peduncular anchors with an anchor bar, while the most advanced have both medial and lateral peduncular anchors; each pair having an anchor bar. Certain families of the Articulonchoinea, the Anchorea n. superord., also have peduncular anchors (parallel evolution): only one family, the Sundanonchidae n. fam., has both medial and lateral peduncular anchors, each anchor pair with an anchor bar. Evolutionary lines from different monogenean evolutionary capacity levels are discussed and a new system of classification for the Monogenea is proposed.In agreeing to publish this article, I recognise that its contents are controversial and contrary to generally accepted views on monogenean systematics and evolution. I have anticipated a reaction to the article by inviting senior workers in the field to comment upon it: their views will be reported in a future issue of this journal. EditorIn agreeing to publish this article, I recognise that its contents are controversial and contrary to generally accepted views on monogenean systematics and evolution. I have anticipated a reaction to the article by inviting senior workers in the field to comment upon it: their views will be reported in a future issue of this journal. Editor     

A new Neocalceostomatid (Monogenoidea) from the gills of the blackfin sea catfish, Arius jella (Siluriformes: Ariidae), in the Bay of Bengal, India

Thysanotohaptor n. gen. (Neocalceostomatidae) is proposed to accommodate Thysanotohaptor rex n. sp. collected from the gills of the blackfin sea catfish Arius jella Day (Siluriformes: Ariidae) from off the coast of Visakhapatnam, Bay of Bengal, Andhra Pradesh, India. Thysanotohaptor is differentiated from the other known neocalceostomatid genera by its species having multiple postgermarial testes (single testis in species of Neocalceostoma and Neocalceostomoides ), lacking a transverse bar associated with the ventral anchor pair (present in species of Neocalceostoma ), and possessing a disc-shaped haptor with a pleated marginal frill (frill absent in Neocalceostomoides spp.; Neocalceostoma spp. with delicate marginal membranes). The Neocalceostomatidae is considered valid within the Order Dactylogyridea based on its members having a haptor armed with 10 marginal and 4 ventral hooks and a germarium having a distal loop prior to uniting with the ootype; the family is not assigned to a suborder of Dactylogyridea because of uncertainty in part about the way in which the distribution of haptoral hooks evolved within the taxon.     

Neotropical monogenea. 13. Rhinonastes pseuodocapsaloideum n. gen., n. sp. (Dactylogyridae, Ancyrocephalinae), a nasal parasite of curimat?, Prochilodus nigricans Agassiz (Cypriniformes, Prochilodontidae), in Brazil

Rhinonastes pseudocapsaloideum n. sp. (Dactylogyridae, Ancyrocephalinae) is described from the nasal cavity of Prochilodus nigricans Agassiz (Cypriniformes, Prochilodontidae) in Brazil. Rhinonastes n. gen. is proposed for species possessing a dextroventral genital pore, a bilobed testis, a ventral C-shaped ovary lying between the 2 testicular lobes, and a disc-shaped haptor armed with a ventral anchor-bar complex and 14 hooks.     

Durettechina beveridgei n. g., n. sp. (Nematoda: Seuratidae) from Antechinus spp. (Dasyuridae: Marsupialia) from Australia

Durettechina beveridgei n. g., n. sp. (Nematoda: Seuratidae) is described from Antechinus flavipes (Dasyuridae) from Victoria and New South Wales. A single female from A. bellus from the Northern Territory may also be D. beveridgei. This new genus is compared with other genera of the Echinonematinae, to which it has been assigned. The genus has a unique body armature and most closely resembles Chabaudechina, in the armature of the cephalic bulb, but has four rather than five rows of hooks, and Linstowinema, in having body hooks on the cuticle of the anterior region, but has 18–22 hooks in each row rather than 14–16. The hooks of Durettechina are also smaller and have a less complex root morphology than those of Linstowinema. Durettechina resembles Seurechina and Chabaudechina in having caudal alae into which papillae extend, but differs from both these genera in the number and arrangement of the caudal papillae, as well as in the body armature. Durettechina, is most different from Bainechina, which has neither hooks on a cephalic bulb nor body hooks on the anterior region nor caudal alae.     

Monogeneans from the gills of glassfishes (Teleostei: Perciformes: Ambassidae) in India, with the proposal of Chandacleidus n. g. (Monogenea: Dactylogyridae)

Chandacleidus n. g. (Monogenea, Dactylogyridae) is proposed to include three species collected from the gills of Indian glassfishes (Ambassidae): Chandacleidus recurvatus (Jain, 1961) n. comb. (syn. Urocleidus recurvatus Jain, 1961) from Chanda nama and C. ranga (new host record) is redescribed; and Chandacleidus saiensis n. sp. and C. lucknowensis n. sp., both from Chanda nama and C. baculis, are described. Chandacleidus n. g. is characterised by species possessing: posteriorly united intestinal caeca; overlapping gonads (testis dorsal to ovary); a counterclockwise male copulatory organ; a grooved accessory piece; a dextro-marginal vaginal pore; a haptor with two lateral flaps and armed with dissimilar dorsal and ventral anchor/bar complexes and 14 similar hooks (dissimilar in size); and hook shanks comprised of two subunits.     

<Emphasis Type="Italic">Spicocleidus namae</Emphasis> n. g., n. sp. (Monogenea: Dactylogyridae) on <Emphasis Type="Italic">Chanda nama</Emphasis> (Hamilton) from Lucknow,India

Spicocleidus n. g. is proposed for S. namae n. sp., a new monogenean collected from the gills of an ambassid, Chanda nama (Ham.), in the River Sai near Lucknow, Uttar Pradesh, India. The new genus is characterised by a pair of modified dorsal anchors (spikes), the absence of a dorsal bar, alate lateral expansion of the anterior haptor and the post-ovarian position of the testis.     

A new diplectanid (Monogenea) genus and species from the gills of the black snook, Centropomus nigrescens (Perciformes: Centropomidae) of the Pacific coast of Mexico

Cornutohaptor nigrescensi n. sp. (Diplectanidae) is described from the gills of the black snook, Centropomus nigrescens (Perciformes: Centropomidae) from the Pacific coast of Mexico. Cornutohaptor n. gen. is proposed for this new species and is characterized by possessing 2 intestinal ceca terminating blindly; a germarium looping right intestinal cecum; bilobed testis; 2 seminal vesicles; 7 pairs of hooks, each with protruding thumb; a grooved ventral bar and coiled male copulatory organ (MCO); an accessory piece comprising a "baglike structure" with an appendage; dorsal bars associated parallelly to body midline; and no adhesive accessory organs on the haptor. Cornutohaptor differs from all confamilial genera by including species with anchors with straight and deep root longest, hook pair 1 reduced in size, MCO with counterclockwise rings, and by the morphology of the accessory piece. Cornutohaptor nigrescensi most closely resembles species of Murraytrema Price, 1937, Lobotrema Tripathi, 1937, and Murraytrematoides Yamaguti, 1958, because of the absence of squamodiscs or lamellodiscs on the haptor and tegumental scales on the posterior portion of the body. Cornutohaptor differs from these genera in the position and number of haptoral bars (2 bars in Lobotrema spp., dorsal bars transversally associated in Murraytrema and Murraytrematoides spp.) and in having a coiled MCO (copulatory organ is a comparatively straight, poorly sclerotized tube in Murraytrematoides spp.). This is the first diplectanid described from a centropomid along the Pacific coast of Mexico.     

Branchotenthes robinoverstreeti n. gen. and n. sp. (Monogenea: Hexabothriidae) from gill filaments of the bowmouth guitarfish,Rhina ancylostoma (Rhynchobatidae), in the Indian Ocean

Branchotenthes robinoverstreeti n. gen. and n. ap. (Monogenea: Hexabothriidae) infects the gill filaments of the bowmouth guitarfish, Rhina ancylostoma Bloch and Schneider, 1801 (Rhynchobatidae) in the southwest Indian Ocean off Trafalgar, South Africa. The new species is most easily distinguished from other hexabothriids by the combination of having a symmetrical haptor, C-shaped haptoral sucker sclerites that are approximately equal in size, haptoral suckers that are equal in size and arranged in 3 tandem pairs that each straddle the longitudinal axis of the haptor, glandular-walled vasa efferentia that are dilated in the distal portion and unite medially before connecting to the vas deferens, a thick-walled male copulatory organ with an oblong proximal portion and an unarmed and finger-like distal portion, parallel vaginae that each possess a thin-walled and sperm-filled proximal portion that is strongly sinuous as well as a thick-walled and musculoglandular distal portion that extends sinuously anteriad, and an egg with a filament at each end. This is the first report of a hexabothriid from asharkfin guitarfish (Rhynchobatidae). A key to the genera of Hexabothriidae is provided.     

Amapacanthus amazonicus n. g., n. sp. (Acanthocephala: Diplosentidae: Allorhadinorhynchinae) from Arius passany and Anableps microleps (Pisces) at Maraca Island off northern Brazil

Amapacanthus amazonicus n. g., n. sp. is described from the intestine of Arius passany (Valenciennes) and Anableps microleps Müller. The most important diagnostic features are: a small globular proboscis armed with 6 diagonal rows of 3 stout hooks; middle hooks conspicuously stouter and larger than anterior ones; terminal hooks as long as middle hooks but straighter and more slender; a double-walled proboscis receptacle; a trunk bearing spines anteriorly; and two tubular cement glands in the males. Amapacanthus n. g. is differentiated from Allorhadinorhynchus, Golvanorhynchus and Slendrorhynchus, the other genera of the Allorhadinorhynchinae, by the presence of a globular proboscis armed with a small number (18) of hooks. A key to the species of the Allorhadinorhynchinae is presented.     

Scomberomorocotyle munroi n. g., n. sp. (Scomberomorocotylinae n. subf.), a thoracocotylid monogenean from Scomberomorus munroi (Scombridae) off Australia and Papua New Guinea

Scomberomorocotyle munroi n. g., n. sp. is described from the gills of Scomberomorus munroi, a Spanish mackerel from the coasts of northern Australia and southern Papua New Guinea. The genus belongs to the suborder Gastrocotylinea because a pair of basal accessory sclerites is present in the clamps. However, the worm does not belong to any of the eight gastrocotylinean families as they are currently recognised. The worm appears to be a member of the Thoracocotylidae, in that the male copulatory organ has relatively weakly developed spines, and that the haptor is one-sided with two rows of clamps. However, the worm differs from all thoracocotylids in that the clamps lack the characteristic lateral rib-like thickenings. To accommodate the new genus and species, the diagnosis of the Thoracocotylidae Price is amended to include worms lacking ribs in their clamps, and a new subfamily, the Scomberomorocotylinae n. subfam., is erected; a key to the four subfamilies which we recognise as valid is provided.     

A description of Cinclotaenia georgievi n. sp. (Cestoda: Dilepididae), a tapeworm from the dipper Cinclus cinclus (L.) (Passeriformes: Cinclidae)

Cinclotaenia sp., described originally by Georgiev & Genov (1985) from the dipper Cinclus cinclus (L.) in Bulgaria, has recently been identified from the same host in the Carpathian Mountains in the Slovak Republic. This tapeworm is considered to be a new species, which is named C. georgievi n. sp. It is characterised by: a scolex armed with 23-27 (predominantly 24-26) hooks in two rows; hooks 30.5-36 microm long, with a blade 10-13.5 microm long and resembling in shape the diorchoid hooks of hymenolepidids; irregularly alternating genital pores with simple genital atria; a slightly conical cirrus armed by small spines of up to 3 microm in length; 24-51 testes posterior to a bi-alate, branched ovary; a gravid uterus filled with egg packets; and eggs with filaments. C. georgievi n. sp. differs from the closely-related C. tarnogradskii (Dinnik, 1927) in the slightly higher number of rostellar hooks, which have longer blades, and a larger cirrus.     

Linstowinema breve n. sp. (Nematoda: Seuratidae) a parasite of Antechinus agilis (Marsupialia: Dasyuridae) from Australia

A new echinonematine nematode, Linstowinema breve sp. n., from the small intestine of the dasyurid marsupial Anthechinus agilis is described. The species is distinguished from its congeners by the possession of the following suite of characters: small size; first and third row of cephalic hooks similar in size; second row larger; 13-15 rows of body hooks without undulating edges on the dilated cuticle of the oesophageal region; oesophagus terminating at the level of the 5th-7th row of body hooks; ten pairs of caudal papillae; a large pair of lateral ad-cloacal papillae extend into small lateral alae. Linstowinema larvae previously recorded from A. agilis may be the same species. A key to species of the genus linstowinema is provided.